SKU: 186004663
ACQUITY UPLC BEH C8 Column, 130Å, 1.7 µm, 3 mm X 30 mm, 1/pk

ACQUITY UPLC BEH C8 Column | 186004663


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Product Description

The ACQUITY BEH C8 sorbent is less retentive compared to the ACQUITY BEH C18 sorbent. A method developer may prefer the speed offered by a less retentive column, while improving peak shape and chromatographic performance. The trifunctionally bonded BEH particles offer the widest usable pH range (1-12), superior low pH stability, and ultra-low column bleed.

Specifications

  • Chemistry

    C8

  • Separation Mode

    Reversed Phase

  • Particle Substrate

    Hybrid

  • pH Range Min

    1 pH

  • pH Range Max

    12 pH

  • Maximum Pressure

    18000 psi (1240 Bar)

  • Endcapped

    Yes

  • Silanol Activity

    Low

  • Particle Shape

    Spherical

  • Particle Size

    1.7 µm

  • Endfitting Type

    Parker-style

  • Pore Size

    130 Å

  • Format

    Column

  • Surface Area

    185

  • System

    UPLC, UHPLC

  • Particle Technology

    BEH

  • USP Classification

    L7

  • Inner Diameter

    3 mm

  • Length

    30 mm

  • Carbon Load

    13 %

  • eCord

    Yes

  • UNSPSC

    41115709

  • Brand

    ACQUITY UPLC

  • Product Type

    Columns

  • Units per Package

    1 pk

Product Support

Documents

Documents



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ACQUITY UPLC BEH C8 Column, 130Å, 1.7 µm, 3 mm X 30 mm, 1/pk

In comparison to the ACQUITY BEH C18 sorbent, the ACQUITY BEH C8 sorbent is less retentive. The speed that a less retentive column offers while enhancing peak shape and chromatographic performance may be preferred by a technique developer. The tri-functionally-bound BEH particles provide the lowest column bleed, the best low pH stability, and the greatest practical pH range (1–12).

The ACQUITY UPLC BEH C18 Column is made to satisfy lab and technique requirements as well as a range of chromatographic applications. The column assists in enhancing the sensitivity, speed, and resolution of the analysis. The ACQUITY UPLC BEH C18 Column can be used to achieve a variety of analytical goals, such as achieving ultra-fast analysis, boosting throughput while retaining resolution, or improving resolution while cutting down on analysis time.

The BEH C8 Columns are made in a cGMP, ISO 9002 accredited facility with ultra-pure reagents specifically for use with ACQUITY UPLCs. Each batch is approved for peptide mapping following chromatographic testing using neutral, acidic, and basic analytes. The results are restricted to precise specification ranges in order to maintain repeatability and uniformity from batch to batch and from column to column. By doing this, you can be sure that the lab equipment you receive offers precise analysis and dependable functioning.

Please browse our website or download brochures to see the complete lists or study equipment to view further products offered by Waters. We advise buying straight from our website so that you can be confident the equipment is genuine Waters. You'll also have access to substantial research and information about all of Waters' goods, and you can quickly shop for lab equipment based on your lab's needs.

You may also be interested in checking out Neutrals QC Reference Material; It is possible to utilize the Neutrals QC Reference Material with any chromatographic systems that have a UV detector. It is meant to serve as a benchmarking standard for systems. There are solely neutral chemicals in the mixture. The QC Reference Material will give you confidence in your results, cut down on troubleshooting and rerun time, and allow you to compare results from different laboratories when used consistently and with control charts. This reference material can be used with many different separation techniques.

What Exactly Does the Term "Elution" Mean?

Elution, or the separation of an antibody from the antigen to which it is bound, is a chromatographic procedure that involves employing a solvent to remove an adsorbed material from a solid adsorbing media. Eluent or eluant is the "carrier" component of the mobile phase used in the procedure, moving the analytes through the chromatograph.